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Rare Metals 2024年第10期43卷 5082-5094页

作者： Jing-Yu Zhou Zhi-Cheng Han Shu Zhao Tao Yang Da-Zhou Yan Hai-Jun Yu Institute of advanced Battery materials and Devices College of Materials Science and EngineeringBeijing University of Technology Key Laboratory of advanced Functional materials Ministry of EducationBeijing University of Technology China ENFI Engineering Corporation National Engineering Research Center of Silicon-Based materials Manufacturing Technology

The pursuit of highly active oxygen evolution reaction （OER） catalysts,especially those free of noble metals,is a focal point in fuel cell *** extensive density functional theory calculations,this study designed and evaluated the activity and stability of singleatom catalysts （SACs） composed of 3d,4d and 5d transition metals supported on tungsten-based MXene for OER *** highlighted the exceptional OER performance of Ni@W2CO2,Rh@W2CO2and Pt@W2CO2,displaying remarkably low overpotentials The catalytic activity of TM@W2CO2SACs exhibited a robust correlation with surface properties,particularly the d-band center index and surface work *** Ni@W2CO2,Rh@W2CO2and Pt@W2CO2emerged as promising candidates for OER and oxygen reduction reaction （ORR） bifunctional catalysis,while Pt@W2CO2and Rh@ W2CO2showed high potential for OER and hydrogen evolution reaction （HER） bifunctional catalysis The effectiveness of tungsten-based MXene as a substrate for non-noble-metal SACs marks a breakthrough in OER catalyst design,driving advancements towards sustainable energy solutions and addressing critical challenges in energy conversion and storage.

关键词： Density functional theory MXene Non-noble metal Oxygen evolution reaction Single-atom catalysts

Catalytic upgrading biomass-derived ethanol and acetic acid into C4 chemicals

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Science China Chemistry 2024年第11期67卷 3588-3613页

作者： Tingting Yan Mengting Zhang Runzhi Yuan Weili Dai college of Science Civil Aviation University of China School of materials Science and Engineering & National Institute for advanced materials Nankai University

Synthesis of value-added chemicals from biomass is an essential strategy to mitigate the global dependency on fossil resources and achieve the aim of carbon neutrality. Thereinto, ethanol and acetic acid are crucial biomass-derived platform ***, catalytic upgrading ethanol and acetic acid into C4 energy-intensive fuels and chemicals via the elongation of carbon backbone has received widespread attention. The primary focus of this review is to systematically describe the recent breakthrough in the conversion of ethanol or acetic acid to C4 chemicals including 1,3-butadiene, n-butenes, isobutene or *** attentions will be given to heterogeneous catalyst design strategies, reaction parameters on the catalytic performance along with the relevant mechanism investigations, as well as their future challenges and opportunities. The present review will provide the detailed insights into the synthesis of C4 chemicals from biomass-derived ethanol and acetic acid and shed a light on the development of highly efficient catalysts.

关键词： ethanol acetic acid C4 chemicals catalytic upgrading aldol condensation

Recent advances in glycerol valorization through electrocatalytic methods

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Tungsten 2024年第4期6卷 696-710页

作者： Hao-Hai Dong Yu-Xin Zhu Yi-Gu Li Jia-Yan Liang Ya Tan Xin-Yue Zhang Hao-Min Jiang Liu Lin Ze-Min Sun Center for advanced materials Research & college of Arts and Sciences Beijing Normal University Department of Chemistry University College London

The recent tremendous growth of biodiesel production from vegetable oils or waste fats has led to increased glycerol accumulation as a by-product of this *** sparked attention towards glycerol use and valorization of this largely available and cheap *** several methods for glycerol valorization,electrochemical glycerol oxidation reaction(EGOR)is an attractive alternative anodic reaction to oxygen evolution reaction for a variety of electrolytic synthesis,due to the low thermodynamic ***,the EGOR at the anode can be coupled with a cathodic hydrogen evolution reaction to achieve efficient energy conversion in an aqueous electrolytic *** review provides a comprehensive summary and critical analysis of glycerol electrochemical oxidation research during the last 5 *** review focuses on the recent development and prospects of electrochemical pathways(indirect or direct routes) for application in the *** particular,the recent development and prospects of using noble and non-noble group metal catalysts for glycerol electro-oxidation are ***,reaction product selectivity analysis and conversion efficiency are also highlighted.

关键词： Active oxygen species Electrocatalytic methods Glycerol Noble metal catalysts Non-noble metal catalysts

Design Strategies for Aqueous Zinc Metal Batteries with High Zinc Utilization: From Metal Anodes to Anode-Free Structures

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Nano-Micro Letters 2024年第4期16卷 305-349页

作者： Xianfu Zhang Long Zhang Xinyuan Jia Wen Song Yongchang Liu School of materials Science and Engineering University of Science and Technology Beijing30 College RoadBeijing 100083People’s Republic of China Beijing advanced Innovation Center for materials Genome Engineering Institute for Advanced Materials and TechnologyState Key Laboratory for Advanced Metals and MaterialsUniversity of Science and Technology BeijingBeijing 100083People’s Republic of China

Aqueous zinc metal batteries(AZMBs)are promising candidates for next-generation energy storage due to the excellent safety, environmental friendliness, natural abundance, high theoretical specific capacity, and low redox potential of zinc(Zn) metal. However,several issues such as dendrite formation, hydrogen evolution, corrosion, and passivation of Zn metal anodes cause irreversible loss of the active materials. To solve these issues, researchers often use large amounts of excess Zn to ensure a continuous supply of active materials for Zn anodes. This leads to the ultralow utilization of Zn anodes and squanders the high energy density of AZMBs. Herein, the design strategies for AZMBs with high Zn utilization are discussed in depth, from utilizing thinner Zn foils to constructing anode-free structures with theoretical Zn utilization of 100%, which provides comprehensive guidelines for further research. Representative methods for calculating the depth of discharge of Zn anodes with different structures are first summarized. The reasonable modification strategies of Zn foil anodes, current collectors with pre-deposited Zn, and anode-free aqueous Zn metal batteries(AF-AZMBs) to improve Zn utilization are then detailed. In particular, the working mechanism of AF-AZMBs is systematically introduced. Finally, the challenges and perspectives for constructing high-utilization Zn anodes are presented.

关键词： Aqueous zinc metal batteries Zinc anodes High zinc utilization Depth of discharge Anode-free structures

Copper-coated Porous Polyimide as Ultralight and Safe Current Collectors for advanced LIBs

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Chinese Journal of Polymer Science 2024年第4期42卷 521-531页

作者： Cun-Sheng Liu Jun-Qi Hu Ting-Ting Mao Song-Yi Liao Ru-Ming Feng Yi-Dong Liu Yong-Gang Min School of materials and energy Guangdong University of TechnologyGuangzhou510006China college of Chemistry and Chemical Engineering Zhongkai University of Agriculture and EngineeringGuangzhou510225China Shanwei Branch of advanced energy Science and Technology Guangdong Laboratory Shanwei516600China

Metallic copper is widely used as current collector(CC) for graphite anode of lithium-ion batteries(LIBs) due to its high electrical conductivity and electrochemical stability. However, the large volume density of commercial copper foil(~8.9 g·cm^(-3)) limits the increase of energy density of battery. Here, copper-coated porous polyimide(Cu@PPI) was prepared by vacuum evaporation as collector for the graphite anode. The sandwich structure connects the copper metal on both sides of the collector with excellent electrical conductivity. Compared to commercial Cu foil, Cu@PPI has lighter mass(≤3.9 mg for disc of 12 mm diameter versus 9.9 mg of ~10 μm Cu foil) and lower volume density(≤3.3 g·cm^(-3)). In addition, the porous structure allows of better adhesion of reactive substances and electrochemical properties than pure Cu foils. It is estimated that the energy density of Cu@PPI should be much higher than that of Cu foil. This strategy should be applicable for other current collectors.

关键词： Copper-coated Vacuum evaporation Porous polyimide(PPI) Current collector(CC) LIBs

Tb(Ⅲ)functionalized MOF based self-calibrating sensor integrated with logic gate operation for efficient epinephrine detection in serum

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Journal of Rare Earths 2024年第5期42卷 987-994,I0006页

作者： Dongsheng Zhao Wenqian Li Rongmei Wen Wencui Li Xin Liu Xiutang Zhang Liming Fan Shanxi Key Laboratory of advanced Carbon Electrode materials Shanxi Coal Mine Water Treatment Technology Innovation CenterSchool of Chemistry and Chemical EngineeringNorth University of ChinaTaiyuan030051China Key Laboratory of advanced energy materials Chemistry(Ministry of Education) College of ChemistryNankai UniversityTianjin300071China

By anchoring Tb^(3+)ions on its free carboxyl groups of the nanocaged NiMOF,a dual-emission self-calibrating sensor of Tb^(3+)@NiMOF was fabricated through coordination post-synthetic modification(PSM)*** Tb^(3+)ions as the secondary fluorescent signal and sensing active sites,Tb^(3+)@NiMOF presents great potentials in visually and efficiently monitoring EPI in serum,with high sensitivity and selectivity,fast response,excellent recyclable,and the low detection limit(LOD,3.06 ng/mL).Furthermore,a tandem combinational logic gate based intelligent detection system was constructed to improve the practicability and convenience of epinephrine(EPI)detection in serum by comparing the light emitted colour with the series standard colour cards preset in the *** work provides a promising approach of developing metal-organic frameworks(MOFs)based self-calibrating sensors for intelligent detection of bioactive molecules.

关键词： Metal-organic framework Post-synthetic modification Self-calibrating sensor Logic gate operation Epinephrine detection Rare earths

Emerging high-entropy strategy: A booster to the development of cathode materials for power batteries

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Journal of advanced Ceramics 2024年第8期13卷 1093-1118页

作者： Liping Huang Jinging Zhu J-Xuan Liu Houzheng Wu Guo-Jun Zhang State Key Laboratory for Modification of Chemical Fibers and Polymer materials Institute of Functional MaterialsCollege of Materials Science and EngineeringDonghua UniversityShanghai 201620China SIAMC advanced materials Cooperation Huzhou 313100China

The coordinated development of new energy vehicles and the energy storage industry has become essential for reducing carbon *** cathode material is the key material that determines the energy density and cost of a power battery,but currently developed and applied cathode materials cannot meet the requirements for high specific capacity,low cost,safety,and good ***-entropy materials(HEMs)are a new type of single-phase material composed of multiple principal elements in equimolar or near-equimolar *** interaction between multiple elements can play an important role in improving the comprehensive properties of the material,which is expected to solve the limitations of battery materials in practical ***,this review provides a comprehensive overview of the current development status and modification strategies of power batteries(lithium-ion batteries(LiBs)and sodium-ion batteries(SIBs)),proposes a high-entropy design strategy,and analyses the structure-activity relationship between the high-entropy effects and battery ***,future research topics related to high-entropy cathode materials,including computational guide design,specific synthesis methods,high-entropy electrochemistry,and high-throughput databases,are *** review aims to provide practical guidance for the development of high-entropy cathode materials for next-generation power batteries.

关键词： cathode materials lithium-ion battery(LIB) sodium-ion battery(SIB) high-entropy strategy

Robust chemo-mechanical stability of additives-free SiO_(2)anode realized by honeycomb nanolattice for high performance Li-ion batteries

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Chinese Chemical Letters 2024年第10期35卷 442-446页

作者： Xinpin Pan Yongjian Cui Zhe Wang Bowen Li Hailong Wang Jian Hao Feng Li Jing Li advanced energy Storage materials Lab School of Materials and New EnergyNingxia UniversityYinchuan 750021China School of Chemistry and Chemical Engineering Ningxia UniversityYinchuan 750021China

Silicon-based anodes including Si,Si Oxand SiO_(2)could deliver ultra-large capacities,but degrade fast owing to huge volume change and low ***,large amounts of elastic binder and conductive additives were composited with nanosized silicon-based materials to yield reasonable cycling stability,which nevertheless not only decrease specific capacity but also induce inhomogeneous lithiation/delithiation as well as uneven stress *** nanolattice has exhibited superior mechanical properties which could be ideal structure for silicon-based anodes,but yet faces challenges in integration of chemical reactivity,conductivity and mechanical ***,we fabricate artificial SiO_(2)honeycomb nanolattice consisting of numerous nanoscale SiO_(2)cells interconnected by through-holes,and conformal coating of highly graphitic carbon on the nanolattice is achieved through in situ catalytic ***,the nanolattice is firmly bonded on Cu substrate through atomic interdiffusion irrespective of surface *** unique structure allows fast charge transportation and homogeneous lithiation/delithiation throughout the micron-meter nanolattice,which results in excellent stability and large reversible capacity over 500 cycles at 1 A/*** results highlight design and constructing artificial nanolattice can be an effective way to prevent chemo-mechanical degradation of silicon-based anode materials.

关键词： Li-ion batteries Nanolattice SiO_(2)anode Stability Conductivity

Biomass-derived porous carbon with single-atomic cobalt toward high-performance aqueous zinc-sulfur batteries at room temperature

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Journal of energy Chemistry 2024年第8期95卷 325-335,I0008页

作者： Shenfei Zhao Xiaoshuai Wu Jiliang Zhang Chunjie Li Zixiang Cui Weihua Hu Ruguang Ma Changming Li Institute for Clean energy&advanced materials School of Materials&EnergySouthwest UniversityChongqing 400715China Institute for materials Science and Devices School of Materials Science and EngineeringSuzhou University of Science and TechnologySuzhou 215009JiangsuChina School of materials Science and Engineering Dalian Jiaotong UniversityDalian 116028LiaoningChina

Aqueous zinc-sulfur batteries at room temperature hold great potential for next-generation energy storage technology due to their low cost,safety and high energy ***,slow reaction kinetics and high activation energy at the sulfur cathode pose great challenges for the practical ***,biomass-derived carbon with single-atomic cobalt sites(MMPC-Co)is synthesized as the cathode in Zn-S *** catalysis of single-atom Co sites greatly promotes the transform of cathode electrolyte interface(CEI)on the cathode surface,while offering accelerated charge transfer rate for high conversion reversibility and large electrochemical surface area(ECSA)for high electrocatalytic ***,the rich pore structure not only physically limits sulfur loss,but also accelerates the transport of zinc *** addition,the large pore volume of MMPC-Co is able to relieve the stress effect caused by the volume expansion of Zn S during charge/discharge cycles,thereby maintaining the stability of electrode ***,the sulfur cathode maintains a high specific capacity of 729.96 m A h g^(-1)after 500 cycles at4 A g^(-1),which is much better than most cathode materials reported in the *** work provides new insights into the design and development of room-temperature aqueous Zn-S batteries.

关键词： Biomass-derived carbon Single-atom catalysts Rich pore structure Sulfur cathode Aqueous zinc-sulfur batteries

Atomically dispersed Ni electrocatalyst for superior urea-assisted water splitting

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Journal of energy Chemistry 2024年第3期90卷 1-6,I0002页

作者： Fang Luo Shuyuan Pan Yuhua Xie Chen Li Yingjie Yu Zehui Yang college of materials Science and Engineering State Key Laboratory of New Textile Materials&Advanced Processing TechnologyWuhan Textile UniversityWuhan 430200China Hubei Hydrogen energy Technology Innovation Center Faculty of Materials Science and ChemistryChina University of GeosciencesWuhan 430074HubeiChina

Urea oxidation reaction(UOR) has been selected as substitution for oxygen evolution reaction ascribing to its low thermodynamic voltage as well as utilization of nickel as ***,we report the formation of nickel single atoms(Ni-SAs) as exceptional bifunctional electrocatalyst toward UOR and hydrogen evolution reaction(HER) in urea-assisted water *** UOR catalysis,Ni-SAs perform a superior catalytic performance than Ni-NP/NC and Pt/C ascribing to the formation of HOO-Ni-N_(4) structure evidenced by in-situ Raman spectroscopy,corresponding to a boosted mass activity by 175-fold at 1.4 V *** than Ni-NP/***,Ni-SAs requires only 450 mV overpotential to obtain HER current density of 500 mA cm^(-2).136 mA cm^(-2) is achieved in urea-assisted water splitting at1.7 V for Ni-SAs,boosted by 5.7 times than Pt/C-IrO_(2) driven water splitting.

关键词： Urea oxidation reaction Hydrogen evolution reaction Nickel single atoms Water splitting